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    NDC 68788-6881-06 Omeprazole 20 mg/1 Details

    Omeprazole 20 mg/1

    Omeprazole is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is OMEPRAZOLE.

    Product Information

    NDC 68788-6881
    Product ID 68788-6881_652067ed-baa7-414e-88a2-599c665749ec
    Associated GPIs 49270060006520
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Omeprazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name OMEPRAZOLE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091672
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-6881-06 (68788688106)

    NDC Package Code 68788-6881-6
    Billing NDC 68788688106
    Package 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-6)
    Marketing Start Date 2017-01-20
    NDC Exclude Flag N
    Pricing Information N/A